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NCT03489902 Clinical Trial

Transvaginal Versus Transobturator Paravaginal Repair

Cystocele Clinical Trial

Official title:
Transvaginal Versus Transobturator Paravaginal Repair Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03489902
Other study ID # TVTOPVR
Secondary ID
Status Completed
Phase N/A
First received March 28, 2018
Last updated April 6, 2018
Start date January 1, 2017
Est. completion date March 1, 2018

Study information
Verified date April 2018
Source Ain Shams Maternity Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Clinical trial comparing the new technique for paravaginal repair versus the traditional technique

Description:

trial comparing the transobturator paravaginal repair versus the traditional technique

Recruitment information / eligibility
Status Completed
Enrollment 40
Est. completion date March 1, 2018
Est. primary completion date December 31, 2017
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria:

paravaginal defect cystocele

midline and paravaginal defect cystocele

Exclusion Criteria:

- uterine descent previous cystocele surgery

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Transobturator Paravaginal Repair
Transobturator application of sutures to the white line in cases needing paravaginal repair
• traditional transvaginal Paravaginal Repair
traditional transvaginal application of sutures to the white line

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Ain Shams Maternity Hospital

Outcome
Type Measure Description Time frame Safety issue
Primary Operative data Operative time 1 day
Secondary Pelvic organ prolapse quantification system Evaluation of the postoperative degree of anterior vaginal wall descent 3 month
Secondary Operative Details blood loss 1 day
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